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Parental depression following the early diagnosis of Cystic Fibrosis : a matched, prospective study.

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Parental depression following the early diagnosis of Cystic Fibrosis : a matched, prospective study. / Glasscoe, Claire A.; Lancaster, Gillian A.; Smyth, Rosalind L. et al.
In: The Journal of Pediatrics, Vol. 150, No. 2, 02.2007, p. 185-191.

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Glasscoe CA, Lancaster GA, Smyth RL, Hill J. Parental depression following the early diagnosis of Cystic Fibrosis : a matched, prospective study. The Journal of Pediatrics. 2007 Feb;150(2):185-191. doi: 10.1016/j.jpeds.2006.11.022

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Glasscoe, Claire A. ; Lancaster, Gillian A. ; Smyth, Rosalind L. et al. / Parental depression following the early diagnosis of Cystic Fibrosis : a matched, prospective study. In: The Journal of Pediatrics. 2007 ; Vol. 150, No. 2. pp. 185-191.

Bibtex

@article{5ad656cdc50f465483baa258f53dd92e,
title = "Parental depression following the early diagnosis of Cystic Fibrosis : a matched, prospective study.",
abstract = "To assess risks for parental depression following the diagnosis of cystic fibrosis (CF) in a child. Study design Matched cohort study in NW England; 45 parental couples with a child diagnosed with CF were compared with 45 control couples matching for age, sex, and position in the family of the index child. The Beck Depression Inventory (BDI-II) with a clinical cut-off ≥13 for dysphoria (mild depression) was the main outcome. A stratified analysis was conducted using the Mantel-Haenszel risk-ratio estimator (RRMH) with eight strata for each of the matching variable combinations. Results Heterogeneity was found within the dataset. Parents with a child with CF ≤9 months of age at baseline had an elevated prospective risk of depression (mothers RRMH [95% confidence interval(CI)] = 2·6[1·05,6·42], fathers RRMH [95%CI] = 2·26 [0·97,5·28]). The absence of a group effect for depression at follow-up after adjusting for the matching (mothers RRMH [95%CI] = 1·1 [0·59,2·05], fathers RRMH [95%CI] = 1·42 [0·66,3·08]) masked this heterogeneity. Conclusion This hypothesis-generating finding suggests that parents may be more vulnerable to depression when their child is diagnosed with a life-shortening condition during the first few months of life. Mood in parents of infants diagnosed early needs to be monitored longitudinally and preventative strategies devised.",
author = "Glasscoe, {Claire A.} and Lancaster, {Gillian A.} and Smyth, {Rosalind L.} and Jonathan Hill",
year = "2007",
month = feb,
doi = "10.1016/j.jpeds.2006.11.022",
language = "English",
volume = "150",
pages = "185--191",
journal = "The Journal of Pediatrics",
issn = "0022-3476",
publisher = "Mosby Inc.",
number = "2",

}

RIS

TY - JOUR

T1 - Parental depression following the early diagnosis of Cystic Fibrosis : a matched, prospective study.

AU - Glasscoe, Claire A.

AU - Lancaster, Gillian A.

AU - Smyth, Rosalind L.

AU - Hill, Jonathan

PY - 2007/2

Y1 - 2007/2

N2 - To assess risks for parental depression following the diagnosis of cystic fibrosis (CF) in a child. Study design Matched cohort study in NW England; 45 parental couples with a child diagnosed with CF were compared with 45 control couples matching for age, sex, and position in the family of the index child. The Beck Depression Inventory (BDI-II) with a clinical cut-off ≥13 for dysphoria (mild depression) was the main outcome. A stratified analysis was conducted using the Mantel-Haenszel risk-ratio estimator (RRMH) with eight strata for each of the matching variable combinations. Results Heterogeneity was found within the dataset. Parents with a child with CF ≤9 months of age at baseline had an elevated prospective risk of depression (mothers RRMH [95% confidence interval(CI)] = 2·6[1·05,6·42], fathers RRMH [95%CI] = 2·26 [0·97,5·28]). The absence of a group effect for depression at follow-up after adjusting for the matching (mothers RRMH [95%CI] = 1·1 [0·59,2·05], fathers RRMH [95%CI] = 1·42 [0·66,3·08]) masked this heterogeneity. Conclusion This hypothesis-generating finding suggests that parents may be more vulnerable to depression when their child is diagnosed with a life-shortening condition during the first few months of life. Mood in parents of infants diagnosed early needs to be monitored longitudinally and preventative strategies devised.

AB - To assess risks for parental depression following the diagnosis of cystic fibrosis (CF) in a child. Study design Matched cohort study in NW England; 45 parental couples with a child diagnosed with CF were compared with 45 control couples matching for age, sex, and position in the family of the index child. The Beck Depression Inventory (BDI-II) with a clinical cut-off ≥13 for dysphoria (mild depression) was the main outcome. A stratified analysis was conducted using the Mantel-Haenszel risk-ratio estimator (RRMH) with eight strata for each of the matching variable combinations. Results Heterogeneity was found within the dataset. Parents with a child with CF ≤9 months of age at baseline had an elevated prospective risk of depression (mothers RRMH [95% confidence interval(CI)] = 2·6[1·05,6·42], fathers RRMH [95%CI] = 2·26 [0·97,5·28]). The absence of a group effect for depression at follow-up after adjusting for the matching (mothers RRMH [95%CI] = 1·1 [0·59,2·05], fathers RRMH [95%CI] = 1·42 [0·66,3·08]) masked this heterogeneity. Conclusion This hypothesis-generating finding suggests that parents may be more vulnerable to depression when their child is diagnosed with a life-shortening condition during the first few months of life. Mood in parents of infants diagnosed early needs to be monitored longitudinally and preventative strategies devised.

U2 - 10.1016/j.jpeds.2006.11.022

DO - 10.1016/j.jpeds.2006.11.022

M3 - Journal article

VL - 150

SP - 185

EP - 191

JO - The Journal of Pediatrics

JF - The Journal of Pediatrics

SN - 0022-3476

IS - 2

ER -